acyclovir sodium, 200 mg, 200mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, For Intravenous Use, Single-Use Bag, Fagron…
Reason Lack of Assurance of Sterility
Class I — High risk. Reasonable probability of serious harm or death.
Crystallization: customer complaints for crystallization in finished product.
Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01, For Intravenous Infusion Only MUST BE DILUTED PRIOR TO USE, packaged in 10 x 10mL Single-Dose Vials per pack NDC 68382-048-10, Rx only, Manufactured by: Cadila Healthcare Ltd., Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534.
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Reason Lack of Assurance of Sterility
Reason Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Reason CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Reason Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Reason Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.
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